Cotton variety FM 9150F

ABSTRACT

A novel cotton variety, designated as FM 9150F, is disclosed. The invention relates to seeds, plants, plant cells, plant tissue, harvested products and cotton lint as well as to hybrid cotton plants and seeds obtained by repeatedly crossing plants of variety FM 9150F with other plants. The invention also relates to plants and varieties produced by the method of essential derivation from plants of FM 9150F and to plants of FM 9150F reproduced by vegetative methods, including but not limited to tissue culture of regenerable cells or tissue from FM 9150F.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/123,390, filed Apr. 8, 2008, and U.S. Provisional Application No. 61/195,594 filed Oct. 8, 2008, the disclosures of each of which are herein incorporated by reference in their entirety.

BACKGROUND OF THE INVENTION

(i) Field of the Invention

This invention relates to the field of plant breeding. More particularly, the invention relates to a variety of cotton designated as FM 9150F, its essentially derived varieties and the hybrid varieties obtained by crossing FM 9150F as a parent line with plants of other varieties or parent lines.

(ii) Description of the Related Art

Cotton is an important, fiber producing crop. Due to the importance of cotton to the textile industry, cotton breeders are increasingly seeking to obtain healthy, good yielding crops of excellent quality.

Cotton is commonly reproduced by self-pollination and fertilization. This type of sexual reproduction facilitates the preservation of plant and variety characteristics during breeding and seed production. The preservation of these characteristics are often important to plant breeders for producing cotton plants having desired traits. Other methods of producing cotton plants having desired traits are also used and include methods such as genetic transformation via Agrobacterium infection or direct transfer by microparticle bombardment. Examples of such methods are disclosed, for example, in U.S. Pub. No. 20090049564, incorporated by reference herein in its entirety.

Due to the environment, the complexity of the structure of genes and location of a gene in the genome, among other factors, it is difficult to predict the phenotypic expression of a particular genotype. In addition, a plant breeder may only apply his skills on the phenotype and not, or in a very limited way, on the level of the genotype. As a result, a particular plant breeder cannot breed the same variety twice using the same parents and the same methodology. Thus, a newly bred variety is an unexpected result of the breeding process. Indeed, each variety contains a unique combination of characteristics.

By carefully choosing the breeding parents, the breeding and selection methods, the testing layout and testing locations, the breeder may breed a particular variety type. In addition, a new variety may be tested in special comparative trials with other existing varieties in order to determine whether the new variety meets the required expectations.

SUMMARY OF THE INVENTION

The invention relates to seeds, plants, plant cells, parts of plants, cotton lint or fiber, and cotton textiles of cotton variety FM 9150F as well as to hybrid cotton plants and seeds obtained by repeatedly crossing plants of FM 9150F with other cotton plants. The invention encompasses plants and plant varieties produced by the method of derivation or essential derivation from plants of FM 9150F and to plants of FM 9150F reproduced by vegetative methods, including but not limited to regeneration of embryogenic cells or tissue of FM 9150F.

DETAILED DESCRIPTION OF THE INVENTION

The invention has been obtained by a general breeding process comprising the steps outlined below. (For reference, see chapter 11, “Breeding Self-Pollinated Crops by Hybridization and Pedigree Selection,” in Briggs and Knowles (1967)).

Parent plants, which have been selected for good agronomic and fiber quality traits are manually crossed in different combinations. The resulting F1 (Filial generation 1) plants are self-fertilized and the resulting F2 generation plants, which show a large variability on account of optimal gene segregation, are planted in a selection field.

These F2 plants are observed during the growing season for health, growth vigor, plant type, plant structure, leaf type, stand ability, flowering, maturity, seed yield, boll type, boll distribution, boll size, fiber yield and fiber quality. Plants are then selected. The selected plants are harvested and the bolls analyzed for fiber characteristics and the seed cleaned and stored. This procedure is repeated in the following growing seasons, whereby the selection and testing units increase from individual plants in the F2, to multiple plant containing ‘lines’ (descending from one mother plant) in the F5 and the number of units decrease from approximately 2500 plants in the F2 to 20 lines in the F5 by selecting about 10-20% of the units in each selection cycle.

The increased size of the units, whereby more seed per unit is available, allows the selection and testing in replicated trials on more than one location with a different environment and a more extensive and accurate analyzing of the fiber quality.

The lines or candidate varieties become genotypically more homozygous and phenotypically more homogeneous by selecting similar plant types within a line and by discarding the so called off-types from the very variable F2 generation on to the final F7 or F8 generation.

Depending on the intermediate results the plant breeder may decide to vary on the procedure as described above such as by accelerating the process by testing a particular line earlier or retesting a line another year. He may also select plants for further crossing with existing parent plants or with other plants resulting from the current selection procedure.

By the method of recurrent backcrossing, as described by Briggs and Knowles, supra, in chapter 13, “The Backcross Method of Breeding,” the breeder may introduce a specific trait or traits into an existing valuable line or variety, while otherwise preserving the unique combination of characteristics of this line or variety. In this crossing method, the valuable parent is recurrently used to cross it at least two or three times with each resulting backcross F1, followed by selection of the recurrent parent plant type, until the phenotype of the resulting F1 is similar or almost identical to the phenotype of the recurrent parent with the addition of the expression of the desired trait or traits.

This method of recurrent backcrossing eventually results in an essentially derived variety, which is predominantly derived from the recurrent parent or initial variety. This method can therefore also be used to get as close as possible to the genetic composition of an existing successful variety. Thus, compared to the recurrent parent the essentially derived variety retains a distinctive trait, which can be any phenotypic trait, with the intention to profit from the qualities of that successful initial variety.

Depending on the number of backcrosses and the efficacy of the selection of the recurrent parent plant type and genotype, which can be supported by the use of molecular markers as described by P. Stam (2003), the genetic conformity with the initial variety of the resulting essentially derived variety may vary between 90% and 100%.

Other than recurrent backcrossing, as described herein, such essentially derived variety may also be obtained by the selection from an initial variety of an induced or natural occurring mutant plant, or of an occurring variant (off-type) plant, or of a somaclonal variant plant, or by genetic transformation of regenerable plant tissue or embryogenic cell cultures of the said initial variety by methods well known to those skilled in the art, such as Agrobacterium-mediated transformation as described by Sakhanokho et al., (2004), Reynaerts et al. (2000), Umbeck et al. (1988) and others. Examples of transgenic events transformed in this way are “LLCotton25,” USDA-APHIS petition 02-042-01p (disclosing expression of a bar coding sequence from Streptomyces hygroscopicus encoding phosphinothricin-acetyl-transferase, operably linked to a cauliflower mosaic virus 35S promoter and 3′ untranslated region from a nopaline synthase gene), “Cot 102,” USDA-APHIS petition 03-155-01p (disclosing expression of the vip3A coding sequence from Bacillus thuringiensis encoding the VIP3A protein, operably linked to the Arabidopsis thaliana actin-2 promoter and the terminator from the Agrobacterium tumefaciens nopaline synthase gene), and “281-24-236,” USDA-APHIS petition 03-036-01p (disclosing expression of the crylF coding sequence from Bacillus thuringiensis encoding the CrylF protein, operably linked to a synthetic promoter containing the Agrobacterium tumefaciens mannopine synthase promoter and four copies of the octopine synthase enhancer from Agrobacterium tumefaciens tumor inducing plasmid pTiAch5 and the bi-directional terminator ORF25 polyA) combined with “3006-210-23,” USDA-APHIS petition 03-036-02p (disclosing expression of the crylAc coding sequence from Bacillus thuringiensis encoding the CrylAc protein, operably linked to the Zea mays ubiquitin 1 promoter and the bi-directional terminator ORF25polyA). Information regarding these and other transgenic events referred to herein may be found at the U.S. Department of Agriculture's (USDA) Animal and Plant Health Inspection Service (APHIS) website. An “Event” is defined as a (artificial) genetic locus that, as a result of genetic engineering, carries a foreign DNA comprising at least one copy of the gene(s) of interest. Other methods of genetic transformation are well known in the art such as microprojectile bombardment. See, e.g., U.S. Publication No. 2009/0049564, which is incorporated by reference herein in its entirety.

The plants selected or transformed retain the unique combination of the characteristics of FM 9150F, except for the characteristics (e.g., one, two, three, four, or five characteristics) changed by the selection of the mutant or variant plant or by the addition of a desired trait via genetic transformation. Therefore, the product of essential derivation (i.e., an essentially derived variety) has the phenotypic characteristics of the initial variety, except for the characteristics that change as a result of the act of derivation. Plants of the essentially derived variety can be used to repeat the process of essential derivation. The result of this process is also a variety essentially derived from said initial variety.

In one embodiment, FM 9150F progeny plants are produced by crossing plants of FM 9150F with other, different or distinct cotton plants, and further selfing or crossing these progeny plants with other, distinct plants and subsequent selection of derived progeny plants. The process of crossing FM 9150F derived progeny plants with itself or other distinct cotton plants and the subsequent selection in the resulting progenies can be repeated up to 7 or 8 times in order to produce FM 9150F derived cotton plants.

FM 9150F has been obtained by introducing the Event MON 88913 (APHIS petition 04-086-01p) via a cross between a donor plant containing this Event and the cotton variety “FM 958” (Plant Variety Protection Number 200100208), followed by three backcrosses of the F1 plants resulting from these crosses, that express the characteristics of FM 958 combined with the Event as described above, with plants of FM 958 and an additional forward cross was made with E0263 (BCSI conventional line). The resulting variety FM 9150F is similar to the existing variety FM 958, but differs by its resistance to the herbicide glyphosate as a result of the surprising expression of the Event MON 88913 in combination with the remainder of the characteristics of FM 958.

Provided herein as embodiments of the invention are seeds, plants, plant cells and parts of plants of the cotton variety FM 9150F. Representative seeds of this variety have been deposited under rule 37 CFR 1.809, under ATCC Accession No. PTA-12923. Plants produced by growing such seeds are provided herein as embodiments of the invention. Also provided herein are pollen or ovules of these plants, as well as a cell or tissue culture of regenerable cells from such plants. In another embodiment, the invention provides for a cotton plant regenerated from such cell or tissue culture, wherein the regenerated plant has the morphological and physiological characteristics of cotton cultivar FM 9150F, as described herein (e.g., Table 1), when grown in the same environmental conditions. In yet another embodiment, the invention provides methods of testing for a plant having the morphological and physiological characteristics of cotton cultivar FM 9150F. In one embodiment, the testing for a plant having the morphological and physiological characteristics of cotton cultivar FM 9150F is performed in the same field, under the same conditions and in the presence of plants of FM 9150F, e.g., plants grown from the seed deposited under ATCC Accession No. PTA-12923. In another embodiment, the characteristics to be tested for are those described herein (e.g., Table 1).

Another embodiment of the invention provides for a method of introducing a desired trait into cotton cultivar FM 9150F comprising: (a) crossing the FM 9150F plants, grown from seed deposited under ATCC Accession No. PTA-12923, with plants of another cotton line that comprise a desired trait to produce F1 progeny plants; (b) selecting F1 progeny plants that have the desired trait to produce selected F1 progeny plants; (c) crossing the selected F1 progeny plants with the FM 9150F plants to produce first backcross progeny plants; (d) selecting for first backcross progeny plants that have the desired trait and the physiological and morphological characteristics of cotton cultivar FM 9150F as described herein (e.g., Table 1), when grown in the same environmental conditions, to produce selected first backcross progeny plants; and (e) repeating steps (c) and (d) at least two times in succession to produce selected third or higher backcross progeny plants that comprise the desired trait and all of the physiological and morphological characteristics of cotton cultivar FM 9150F as described herein (e.g., Table 1), when grown in the same environmental conditions. Plants produced by this method have all of the physiological and morphological characteristics of FM 9150F, except for the characteristics derived from the desired trait.

Another embodiment of the invention provides for a method of producing an essentially derived plant of cotton variety FM 9150F comprising introducing a transgene conferring the desired trait into the plant. In another embodiment, the invention provides for a method of producing an essentially derived cotton plant from FM 9150F comprising genetically transforming a desired trait in regenerable cell or tissue culture from a plant produced by the invention, resulting in an essentially derived cotton plant that retains the expression of the phenotypic characteristics of cotton variety FM 9150F, except for the characteristics changed by the introduction of the desired trait.

Desired traits described herein include modified cotton fiber characteristics, herbicide resistance, insect resistance, bacterial disease resistance, fungal disease resistance, male sterility, modified carbohydrate metabolism and modified fatty acid metabolism. Such traits and genes conferring such traits are known in the art. See, e.g., US 20090049564, incorporated by reference herein in its entirety.

The invention also provides for methods wherein the desired trait is herbicide tolerance and the tolerance is linked to a herbicide such as glyphosate, glyfosinate, sulfonylurea, dicamba, phenoxy proprionic acid, cycloshexone, triazine, benzonitrile, bromoxynil or imidazalinone. The invention also provides for methods wherein the herbicide tolerance is an expression of the Event “LLCotton25” and the insect resistance is an expression of the Event “281-24-236”, Event “3006-210-23” or a combination thereof, or Event “Cot 102”.

Also included herein is a method of producing cotton seed, comprising the steps of using the plant grown from seed of cotton variety FM 9150F, of which a representative seed sample has been deposited under ATCC Accession No. PTA-12923, as a recurrent parent in crosses with other cotton plants different from FM 9150F, and harvesting the resultant cotton seed.

Another embodiment of this invention relates to seeds, plants, plant cells and parts of plants of cotton varieties that are essentially derived from FM 9150F, being essentially the same as this invention by expressing the unique combination of characteristics of FM 9150F, including the herbicide resistance of FM 9150F, except for the characteristics (e.g., one, two, three, four, or five characteristics) being different from the characteristics of FM 9150F as a result of the act of derivation.

Another embodiment of this invention is the reproduction of plants of FM 9150F by the method of tissue culture from any regenerable plant tissue obtained from plants of this invention. Plants reproduced by this method express the specific combination of characteristics of this invention and fall within its scope. During one of the steps of the reproduction process via tissue culture somaclonal, variant plants may occur. These plants can be selected as being distinct from this invention, but still fall within the scope of this invention as being essentially derived from this invention.

Another embodiment of this invention is the production of a hybrid variety comprising repeatedly crossing plants of FM 9150F with plants of a different variety or varieties or with plants of a non-released line or lines. In practice, three different types of hybrid varieties may be produced (see, e.g., Chapter 18, “Hybrid Varieties” in Briggs and Knowles, supra):

The “single cross hybrid” produced by two different lines, the “three way hybrid,” produced by three different lines such that first the single hybrid is produced by using two out of the three lines followed by crossing this single hybrid with the third line, and the “four way hybrid” produced by four different lines such that first two single hybrids are produced using the lines two by two, followed by crossing the two single hybrids so produced.

Each single, three way or four way hybrid variety so produced and using FM 9150F as one of the parent lines contains an essential contribution of FM 9150F to the resulting hybrid variety and falls within the scope of this invention.

The invention also provides for cotton lint or fiber produced by the plants of the invention, plants reproduced from the invention, and plants essentially derived from the invention. The final textile produced from the unique fiber of FM 9150F also falls within the scope of this invention. The invention also provides for a method of producing a commodity plant product (e.g., lint, cotton seed oil) comprising obtaining a plant of the invention or a part thereof, and producing said commodity plant product thereform.

The entire disclosure of each document cited herein (e.g., US patent publications, non-patent literature, etc.) is hereby incorporated by reference.

Deposit Information

A representative sample of at least 2500 seeds of FM 9150F has been deposited with the American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, VA 20110, USA, under ATCC Accession No. PTA-12923. The seeds were deposited with the ATCC on May 23, 2012, under the Budapest Treaty.

EXAMPLE 1

Seeds were obtained from plants finally selected in the process of breeding the new variety “FM 9150F”.

Seeds of the variety FM 9150F, of which a representative sample will be deposited, were planted, together with seeds of cotton variety FM 958 as reference variety, in field trials at two locations, as discussed hereunder.

The results as shown in Tables 1-4 were obtained from a pooled analysis of the data from these two trials.

1. BCS Research Station, Office location, Lubbock, TX 2006-2007. Conditions: trial was conducted in the field under irrigation with conventional management. Trial design for distinguishing characters: random complete block design with six replications and two 14 m row plots. For distinguishing characters: measurements were taken from 10 plants, from each of the 14 m plots.

2. BCS Research Clark location, Lubbock, TX 2006-2007. Conditions: trial was conducted in the field under irrigation with conventional management. Trial design for distinguishing characters: random complete block design with six replications and two 14 m row plots. For distinguishing characters: measurements were taken from 10 plants, from each of the 14 m plots.

Analysis of variance procedures were used to obtain least significant difference at the 5% level, using Agrobase software.

Tables 1-4 reflect the average expression of the characteristics of FM 9150F on these locations in 2006 and 2007. This expression can be different on other locations and/or in other years. The sample that will be deposited represents the variety and this sample can be analyzed for the expression of its phenotypic characteristics at any time and at any location.

FM 9150F is most similar and closely resembles FM 958, but can be distinguished from its comparator varieties by the following: FM 9150F contains the single transgene MON 88913 from Monsanto Corp. while FM 958 does not; FM 9150F mature plant height is less than FM 958; FM 9150F has a lower seed index than FM 958; FM 9150F has a higher gin turnout than that of FM 958; FM 9150F has a longer fiber length, but less uniformity than FM 958; FM 9150F has a stronger fiber than FM 958; FM 9150F has a tower micronaire than both FM 958.

TABLE 1 Characteristics of FM 9150F Description of Variety Characteristic Possible Expression/Note FM 9150F FM 958 General Plant Type Plant Habit spreading, Compact Compact intermediate, compact Foliage sparse, intermediate, Intermediate Intermediate dense Stem Lodging lodging, intermediate, Erect Erect erect Fruiting Branch clustered, short, Normal Normal normal Growth determinate, inter- Intermediate Intermediate mediate, indeterminate Leaf color greenish yellow, light Medium Medium green, medium green, Green Green dark green Boll Shape Length < Width, L = Length > Length > W, L > W Width Width Boll Breadth broadest at base, Base Base broadest at middle Maturity date of 50% open bolls Early Early Plant cm. to first from cotyledonary 20.6 20.1 Fruiting Branch node No. of nodes to 1st excluding cotyledonary 7.5 7.3 Fruiting Branch node Mature Plant Height cotyledonary node to 55 57 in cm. terminal Leaf: upper most, fully expanded leaf Type normal, sub-okra, okra, Normal Normal super-okra Pubescense absent, sparse, Medium Medium medium, dense Nectaries present, absent Present Present Stem Pubescense glabrous, intermediate, Intermediate Intermediate hairy Glands (Gossypol) absent, sparse, normal, more than normal Leaf Normal Normal Stem Normal Normal Calyx lobe (normal is absent) Absent/ Normal Normal Flower Petals cream, yellow Cream Cream Pollen cream, yellow Cream Cream Petal Spot present, absent Absent Absent Seed Seed Index g/100 seed fuzzy basis 10.9 11.2 Lint Index g lint/100 seeds Boll Lint percent, picked 42.8 42.5 Gin Turnout, stripped 31 30.5 Number of Seeds per Boll Grams Seed Cotton per Boll Number of Locules 4.5 4.5 per Boll Boll Type storm proof, storm Storm Storm resistant, open Resistant Resistant Fiber Properties Method HVI Length, inches, 2.5% 1.21 1.19 SL Uniformity (%) 82.3 83 Strength, T1 (g/tex) 30.5 29.8 Elongation, E1 (%) 4.6 5.3 Micronaire 3.9 4.2 Diseases, Insects and Pests Bacterial Blight susceptible = S, race 1 moderately Bacterial Blight susceptible = MS race 2 Bacterial Blight Race moderately resistant = 18 MR, resistant = R Verticillium Wilt Bollworm Cotton Leafworm Fall Armyworm Pink Bollworm Tobacco Budworm

TABLE 2 PLANT MEASUREMENT ANALYSIS LOCKS_BOLL SEED_INDEX HT ENTRY_NAME (number) (grams) CMFB (cm) NFB (cm) (cm) FM 9150F 4.5 10.9 20.6 7.5 55.0 FM 958 4.5 11.2 20.1 7.3 57.0

TABLE 3 LBS LINT/ACRE ENTRY MEAN % MEAN NAME LINT GIN TURNOUT LOCS OFFICE CLARK PATSCHKE SIDES GAINES INADALE MELCHER TULIA FM 9150F 42.8 31 1106 1240 681 641 1492 1707 896 1107 1084 FM 958 42.5 30.5 1123 1314 863 774 1439 1541 831 1096 1128 P > T* 0.253 0.109 0.935 *Probability associated with a Student's paired t-Test, with a two-tailed distribution (0.196016)

TABLE 4 FIBER AND VISUAL DATA ACROSS ALL LOCATIONS MEAN HVI FIBER QUALITY PLANT_HT STORM VISUAL MATURITY LEN UNIF STREN ELONG ENTRY NAME (in) RESISTANCE RATING VISUAL (in) (%) (g/tex) (%) MIC FM 9150F 29.3 5.9 6.7 34.2 1.21 82.3 30.50 4.6 3.9 FM 958 29.7 5.2 7.0 25.0 1.19 83.0 29.8 5.3 4.2 P > T* 0.523 0.016 0.147 0.709 0.029 0.240 0.3100 0.005 4.200 *Probability associated with a Student's paired t-Test, with a two-tailed distribution (0.196016)

EXAMPLE 2

A variety that has been essentially derived from FM 9150F by the process of the transgression of the Event LLCotton 25, USDA-APHIS petition 02-042-01p, U.S. Pat. No. 6,818,807, into plants of the variety FM 9150F via the method of recurrent backcrossing and selecting the plants which express the characteristics of FM 9150F combined with the resistance to the herbicide glyfosinate.

EXAMPLE 3

A variety that has been essentially derived from FM 9150F by the process of the transgression of the Event LLCotton 25 via genetic engineering in regenerable cells or tissue of FM 9150F and the subsequent selection of regenerated plants, which express the characteristics of FM 9150F combined with the resistance to the herbicide glyfosinate.

EXAMPLE 4

A variety that has been essentially derived from FM 9150F by the selection of an induced or natural occurring mutant plant or off-type plant from plants of FM 9150F, which plant retains the expression of the phenotypic characteristics of FM 9150F and differs only from FM 9150F in the expression of one, or two, or three, or four, or five of the characteristics as listed in Table 1, and when grown side-by-side with FM 9150F on one or two locations in one or two growing seasons.

Cited References

Lawrence P. Burdett, “Cotton Variety 02T15.” U.S. Pub. No. 20090049564.

F. N. Briggs and P. F. Knowles, “Introduction to Plant Breeding.” Rheinhold Publishing Corporation, 1967.

H. F. Sakhanoko et al., “Induction of Somatic Embryogenesis and Plant Regeneration in Select Georgia and Pee Dee Cotton Lines.” Crop Science 44: 2199-2205 (2004).

Umbeck et al., “Genetic Engineering of Cotton Plants and Lines.” Published patent Application Number EP0290355 (1988).

Reynaerts et al., “Improved Method for Agrobacterium Mediated Transformation of Cotton.” International Publication Number WO 00/71733 (2000).

P. Stam, “Marker-assisted introgression: speed at any cost?” Proceedings of the Eucarpia Meeting on Leafy Vegetable Genetics and Breeding, Noordwijkerhout, The Netherlands, 19-21 Mar. 2003. Eds. Th. J. L. van Hintum, A. Lebeda, D. Pink, J. W. Schut. P117-124 (2003).

Trolinder et al. “Herbicide tolerant cotton plants having event EE-GH1.” U.S. Pat. No. 6,818,807 (2004). 

1. A seed of cotton variety FM 9150F, wherein a representative sample of seed of said variety has been deposited under ATCC Accession No. PTA-12923.
 2. A plant, or part thereof, produced by growing the seed of claim
 1. 3. The plant part of claim 2, wherein said plant part is pollen, an ovule or a cell.
 4. A seed produced by the plant of claim
 2. 5. A plant, or part thereof, obtained by vegetative reproduction from the plant or part thereof of claim 2, said plant or part thereof expressing all phenotypic characteristics of cotton variety FM 9150F.
 6. A method of vegetative reproduction of cotton variety FM 9150F comprising culturing regenerable cells or tissue from FM 9150F.
 7. A cell or tissue culture produced from the plant or part thereof of claim
 2. 8. A cotton plant regenerated from the cell or tissue culture of claim 7, expressing all phenotypic characteristics of FM 9150F.
 9. A method of producing F1 hybrid cotton seed, comprising crossing the plant of claim 2 with a cotton plant distinct from FM 9150F, and harvesting the resultant F1 hybrid cotton seed.
 10. A F1 hybrid cotton seed produced by the method of claim
 9. 11. A F1 hybrid cotton plant, or part thereof, produced by growing the seed of claim
 10. 12. A plant obtained by the vegative reproduction of the plant of claim 11, expressing all phenotypic characteristics of the plant of claim
 11. 13. A method of producing F1 cotton seed comprising crossing the plant of claim 11 with a cotton plant distinct from the plant of claim 11, and harvesting the resultant F1 hybrid cotton seed.
 14. A method of producing an essentially derived cotton plant from FM 9150F, comprising introducing a transgene conferring a desired trait into the plant of claim
 2. 15. A method of producing essentially derived cotton plant from FM 9150F comprising backcrossing the plant of claim 2 at least two times to obtain an essentially derived cotton plant from FM 9150F, said essentially derived cotton plant retaining the expression of the phenotypic characteristics of FM 9150F, except for those characteristics changed by said backcrossing.
 16. The method of claim 14, wherein the desired trait is modified cotton fiber characteristics, herbicide tolerance, insect resistance, bacterial disease resistance, fungal disease resistance, male sterility, modified carbohydrate metabolism or modified fatty acid metabolism.
 17. The method of claim 16, wherein the desired trait is herbicide tolerance and the tolerance to the herbicide of glyphosate, glyfosinate, sulfonylurea, dicamba, phenoxy proprionic acid, cycloshexone, triazine, benzonitrile, bromoxynil or imidazalinone is conferred.
 18. The method of claim 16, wherein the herbicide tolerance is an expression of a bar coding sequence from Streptomyces hyproscopicus encoding phosphinothricin-acetyl-transferase, operably linked to a cauliflower mosaic virus 35S promoter and 3′ untranslated region from a nopaline synthase gene and the insect resistance is an expression of a) the cry1F coding sequence from Bacillus thurigiensis encoding the Cry1F protein, operably linked to a synthetic promoter containing the Agrobacterium tumefaciens mannopine synthase promoter and four copies of the octopine synthase enhancer from Agrobacterium tumefaciens tumor inducing plasmid pTiAch5 and the bi-directional terminator ORF25 polyA; b) the cry1Ac coding sequence from Bacillus thuringiensis encoding the Cry1Ac protein, operably linked to the Zea mays ubiquitin 1 promoter and the bi-directional terminator ORF25 polyA; c) a combination of a) and b); or d) the vip3A coding sequence from Bacillus thuringiensis encoding the VIP3A protein, operably linked to the Arabidopsis thaliana actin-2 promoter and the terminator from the Agrobacterium tumefaciens nopaline synthase gene.
 19. A method of producing essentially derived cotton plants, comprising selecting a mutant or variant plant from the plant of claim 2; producing a regenerable cell or tissue culture from the selected plant; and genetically transforming a desired trait into the regenerable plant cell or plant tissue, resulting in an essentially derived cotton plant that retains the phenotypic characteristics of cotton variety FM 9150F, except for the characteristics changed by the selection of the mutant or variant plant and the characteristics changed by the introduction of the desired trait.
 20. A plant, or part thereof, produced by the method of claim 14, which retains the phenotypic characteristics of cotton variety FM 9150F, including a herbicide resistance characteristic of the expression of the Event “MON88913”, except for the characteristics changed by the introduction of the desired trait.
 21. A method of producing a cotton plant derived from cotton variety FM 9150F, comprising a) crossing the plant of claim 2 with another cotton plant distinct from the plant of claim 2; b) growing the resulting F1 seed to obtain a F1 plant and crossing the F1 plant with itself or with another, distinct cotton plant to obtain progeny seed; and c) growing the progeny seed of step b) to obtain a progeny plant and crossing the progeny plant with itself or with another, distinct cotton plant, thereby producing a FM 9150F derived cotton plant.
 22. The method of claim 21, further comprising repeating step c) up to eight times. 